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Erlotinib (Tarceva (Trademark), OSI-774) in Treating Patients with Advanced Non-Small Cell Lung Cancer

This trial is complete
The study has ended normally, and participants are no longer being examined or treated (that is, the last participant's last visit has occurred).

Clinicaltrials.gov ID

The unique identification code given to each clinical study upon registration at ClinicalTrials.gov.
NCT00072631

Astellas Study ID

The unique identification code given by the study sponsor.

OSI-774-202

EudraCT ID

The unique identification code given to each clinical study upon registration at EudraCT (European Union Drug Regulating Authorities Clinical Trials Database).

Dose to Rash

Follow Trial

Condition

Non Small Cell Lung Cancer, Advanced/Metastatic Cancer

Phase

These clinical trials are done to learn if an experimental treatment helps participants who have a specific condition or disease. Phase 2 trials usually include a larger group of participants than Phase 1 trials.

Phase 2

Age

18 Years - N/A N/A

Sex

Female & Male

Product

N/A

Type

A type of clinical study in which participants are assigned to groups that receive one or more intervention/treatment (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.

Interventional

Trial Dates

Nov 2003 - Mar 2007

Masking

None (Open Label)

Enrollment number

43

A Phase II, Open-label, Intra-patient Dose-escalation Study of Erlotinib in Patients with Advanced Non-small Cell Lung Cancer who have Failed Prior Chemotherapy

Study summary

Study documents

Study Documents, including study results, are available after a study is completed or terminated, according to Astellas Transparency policy.

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Locations

Institute for Drug Development Cancer Therapy and Research Center

San Antonio, United States, 78229

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